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Use of RDS MultiSense® in Post-ICU Patients in the COVID-19 Era

NCT04661423 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2025-05-01

No results posted yet for this study

Summary

In this clinical study, the investigators will compare vital parameters measurements obtained using continuous data from reference monitors and continuous wireless MultiSense® monitoring patch in 60 post-ICU (Intensive Care Unit) patients and over 7 days.

Conditions

  • Post ICU Rehabilitation

Interventions

OTHER

Remote Automated Monitoring System

The patient will be monitored with conventional monitoring devices as well as the MultiSense patch.

Sponsors & Collaborators

  • Rhythm Diagnostic Systems

    collaborator INDUSTRY

  • IHU Strasbourg

    lead OTHER

Principal Investigators

  • Julien POTTECHER, MD, PhD · Anesthesia, Critical Care & Perioperative Medicine, Hautepierre, Strasbourg, France

Study Design

Allocation
NA
Purpose
OTHER
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-09-02
Primary Completion
2025-03-02
Completion
2025-03-02

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04661423 on ClinicalTrials.gov